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1 Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, Kansas 66160-7401; 2 Department of Medicine, University of California, San Diego, La Jolla, California 92093-0623; and 3 Functional Genomics Laboratory, Medical College of Ohio, Toledo, Ohio 43614-5804
O2 transport
during maximal exercise was studied in rats bred for extremes of
exercise endurance, to determine whether maximal O2 uptake
(
O2 max) was different in high- (HCR)
and low-capacity runners (LCR) and, if so, which were the phenotypes
responsible for the difference.
O2 max
was determined in five HCR and six LCR female rats by use of a
progressive treadmill exercise protocol at inspired
PO2 of ~145 (normoxia) and ~70 Torr
(hypoxia). Normoxic
O2 max (in
ml · min
1 · kg
1)
was 64.4 ± 0.4 and 57.6 ± 1.5 (P < 0.05),
whereas
O2 max in hypoxia was 42.7 ± 0.8 and 35.3 ± 1.5 (P < 0.05) in HCR and LCR,
respectively. Lack of significant differences between HCR and LCR in
alveolar ventilation, alveolar-to-arterial PO2
difference, or lung O2 diffusing capacity indicated that
neither ventilation nor efficacy of gas exchange contributed to the
difference in
O2 max between groups.
Maximal rate of blood O2 convection (cardiac output times
arterial blood O2 content) was also similar in both groups.
The major difference observed was in capillary-to-tissue O2
transfer: both the O2 extraction ratio (0.81 ± 0.002 in HCR, 0.74 ± 0.009 in LCR, P < 0.001) and the
tissue diffusion capacity (1.18 ± 0.09 in HCR and 0.92 ± 0.05 ml · min
1 · kg
1 · Torr
1
in LCR, P < 0.01) were significantly higher in HCR.
The data indicate that selective breeding for exercise endurance
resulted in higher
O2 max mostly
associated with a higher transfer of O2 at the tissue level.
O2 transport; lung diffusion capacity; muscle diffusion capacity; genetic models
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